WO2006065711A3 - Antagonistes du recepteur de tachykinine d'octahydropyrano[3,4-c]pyrrole - Google Patents

Antagonistes du recepteur de tachykinine d'octahydropyrano[3,4-c]pyrrole Download PDF

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Publication number
WO2006065711A3
WO2006065711A3 PCT/US2005/044822 US2005044822W WO2006065711A3 WO 2006065711 A3 WO2006065711 A3 WO 2006065711A3 US 2005044822 W US2005044822 W US 2005044822W WO 2006065711 A3 WO2006065711 A3 WO 2006065711A3
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WIPO (PCT)
Prior art keywords
receptor antagonists
octahydropyrano
pyrrole
compounds
tachykinin receptor
Prior art date
Application number
PCT/US2005/044822
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English (en)
Other versions
WO2006065711A2 (fr
Inventor
Robert J Devita
Jinlong Jiang
Sander G Mills
Jonathan R Young
Original Assignee
Merck & Co Inc
Robert J Devita
Jinlong Jiang
Sander G Mills
Jonathan R Young
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Publication date
Application filed by Merck & Co Inc, Robert J Devita, Jinlong Jiang, Sander G Mills, Jonathan R Young filed Critical Merck & Co Inc
Priority to CA002590039A priority Critical patent/CA2590039A1/fr
Priority to AU2005316676A priority patent/AU2005316676A1/en
Priority to JP2007546800A priority patent/JP2008523147A/ja
Priority to US11/792,514 priority patent/US7652058B2/en
Priority to EP05853689A priority patent/EP1827420A4/fr
Publication of WO2006065711A2 publication Critical patent/WO2006065711A2/fr
Publication of WO2006065711A3 publication Critical patent/WO2006065711A3/fr

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
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  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Pulmonology (AREA)
  • Psychiatry (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Cardiology (AREA)
  • Dermatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Otolaryngology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Rheumatology (AREA)
  • Hospice & Palliative Care (AREA)
  • Ophthalmology & Optometry (AREA)
  • Vascular Medicine (AREA)
  • Transplantation (AREA)
  • Toxicology (AREA)
  • Psychology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

La présente invention se rapporte à certains composés d'hydropyranopyrrolidine, utiles comme antagonistes du récepteur de la neurokinine-1 (NK-1) et comme inhibiteurs de la tachykinine, en particulier de la substance P. Cette invention concerne également des formulations pharmaceutiques comprenant ces composés comme ingrédients actifs ainsi que l'utilisation de ces composés et de leurs formulations dans le traitement de certains troubles, parmi lesquels figurent le vomissement, l'incontinence urinaire, la dépression et l'anxiété.
PCT/US2005/044822 2004-12-14 2005-12-12 Antagonistes du recepteur de tachykinine d'octahydropyrano[3,4-c]pyrrole WO2006065711A2 (fr)

Priority Applications (5)

Application Number Priority Date Filing Date Title
CA002590039A CA2590039A1 (fr) 2004-12-14 2005-12-12 Antagonistes du recepteur de tachykinine d'octahydropyrano[3,4-c]pyrrole
AU2005316676A AU2005316676A1 (en) 2004-12-14 2005-12-12 Octahydropyrano[3,4-c]pyrrole tachykinin receptor antagonists
JP2007546800A JP2008523147A (ja) 2004-12-14 2005-12-12 オクタヒドロピラノ[3,4−c]ピロールタキキニン受容体拮抗薬
US11/792,514 US7652058B2 (en) 2004-12-14 2005-12-12 Octahydropyrano[3,4-C]pyrrole tachykinin receptor antagonists
EP05853689A EP1827420A4 (fr) 2004-12-14 2005-12-12 Antagonistes du recepteur de tachykinine d'octahydropyrano[3,4-c]pyrrole

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US63577704P 2004-12-14 2004-12-14
US60/635,777 2004-12-14
US63806504P 2004-12-20 2004-12-20
US60/638,065 2004-12-20

Publications (2)

Publication Number Publication Date
WO2006065711A2 WO2006065711A2 (fr) 2006-06-22
WO2006065711A3 true WO2006065711A3 (fr) 2006-08-31

Family

ID=36588419

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2005/044822 WO2006065711A2 (fr) 2004-12-14 2005-12-12 Antagonistes du recepteur de tachykinine d'octahydropyrano[3,4-c]pyrrole

Country Status (6)

Country Link
US (1) US7652058B2 (fr)
EP (1) EP1827420A4 (fr)
JP (1) JP2008523147A (fr)
AU (1) AU2005316676A1 (fr)
CA (1) CA2590039A1 (fr)
WO (1) WO2006065711A2 (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007075528A2 (fr) * 2005-12-22 2007-07-05 Merck & Co., Inc. Antagonistes de recepteur d’octahydropyrano[3,4-c]pyrrole-tachykinine
US8124633B2 (en) * 2007-04-10 2012-02-28 Merck Sharp & Dohme Corp. Hydroxymethyl ether hydroisoindoline tachykinin receptor antagonists
WO2009002770A1 (fr) * 2007-06-22 2008-12-31 Merck & Co., Inc. Antagonistes 6,5-pyrrolopipéridine des récepteurs de tachykinine
ES2672099T3 (es) 2011-07-04 2018-06-12 Irbm - Science Park S.P.A. Antagonistas del receptor NK-1 para el tratamiento de la neovascularización corneal
MX2014010012A (es) * 2012-02-22 2014-09-12 Leo Pharma As Nuevos compuestos antagonistas del receptor de neurocinina 1.
EP3758688B1 (fr) 2018-02-26 2024-03-27 Ospedale San Raffaele S.r.l. Antagonistes nk-1 destinés à être utilisés dans le traitement de la douleur oculaire
EP3870572A1 (fr) * 2018-10-23 2021-09-01 Myelopro Diagnostics and Research GmbH Composés ciblant la calréticuline mutante
US20230134843A1 (en) 2020-03-11 2023-05-04 Ospedale San Raffaele S.R.L. Treatment of stem cell deficiency

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4535169A (en) * 1983-09-12 1985-08-13 The Board Of Trustees Of The University Of Illinois 5H-6-oxo-2,3,4,4a,7,7a-hexahydropyrano[2,3-b]pyrrole and the preparation thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU722883B2 (en) * 1995-10-18 2000-08-10 Merck & Co., Inc. Cyclopentyl tachykinin receptor antagonists
TWI341198B (en) * 2004-01-27 2011-05-01 Merck Sharp & Dohme Hydroisoindoline tachykinin receptor antagonists

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4535169A (en) * 1983-09-12 1985-08-13 The Board Of Trustees Of The University Of Illinois 5H-6-oxo-2,3,4,4a,7,7a-hexahydropyrano[2,3-b]pyrrole and the preparation thereof

Also Published As

Publication number Publication date
AU2005316676A1 (en) 2006-06-22
EP1827420A2 (fr) 2007-09-05
US20080108689A1 (en) 2008-05-08
WO2006065711A2 (fr) 2006-06-22
EP1827420A4 (fr) 2009-03-04
CA2590039A1 (fr) 2006-06-22
JP2008523147A (ja) 2008-07-03
US7652058B2 (en) 2010-01-26

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